Scheidt S
Division of Cardiology, New York Hospital-Cornell Medical Center, NY 10021.
Am Heart J. 1988 Jul;116(1 Pt 1):254-9. doi: 10.1016/0002-8703(88)90286-4.
Nicardipine is a new dihydropyridine calcium channel blocking drug with actions that suggest considerable usefulness as an agent for chronic stable angina. Hemodynamic studies in patients with coronary artery disease confirm major coronary vasodilator actions, perhaps even exceeding its considerable systemic vasodilator properties with little or no negative inotropic effect. Three recent controlled clinical trials that used nicardipine alone suggest approximately 20% to 30% increase in exercise time, and at least that much decrease in anginal episodes and sublingual nitroglycerin consumption when compared with placebo in doses of 90 to 120 mg daily. Five trials comparing nicardipine with other calcium channel blockers, and three with beta blockers, suggest equivalent efficacy, including decrease in angina and increase in exercise time. Adverse effects of nicardipine generally relate to its potent vasodilatory capability and are usually minor. Side effects are frequent at the beginning of many trials, usually do not cause undue withdrawals, and are quite rare after 6 to 12 months on the drug in most studies.
尼卡地平是一种新型二氢吡啶类钙通道阻滞剂,其作用表明它作为慢性稳定性心绞痛的治疗药物具有很大的应用价值。对冠心病患者的血流动力学研究证实,它具有主要的冠状动脉舒张作用,甚至可能超过其显著的全身血管舒张特性,且几乎没有负性肌力作用。最近三项单独使用尼卡地平的对照临床试验表明,与安慰剂相比,每日服用90至120毫克尼卡地平可使运动时间增加约20%至30%,心绞痛发作次数和舌下硝酸甘油消耗量至少减少同样幅度。五项比较尼卡地平和其他钙通道阻滞剂的试验,以及三项比较尼卡地平和β受体阻滞剂的试验,表明它们具有等效疗效,包括减少心绞痛发作和增加运动时间。尼卡地平的不良反应通常与其强大的血管舒张能力有关,且一般较轻。在许多试验开始时副作用较为常见,通常不会导致过多患者退出试验,并且在大多数研究中,服用该药物6至12个月后副作用相当罕见。